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Aniline Nitrate
There's a slight confusion here. You are trying to make aniline nitrate the salt (PhNH[sub]3[/sub][s ...
22-12-2017 at 22:44
by: kavu
Four thieves vinegar
[rquote=494686&tid=77526&author=Assured Fish]
[quote]
There are plenty of examples where m ...
15-10-2017 at 04:41
by: kavu
Four thieves vinegar
Drug synthesis is complicated by the purity requirements for all stages including the final API. The ...
14-10-2017 at 22:07
by: kavu
Geosmin synthesis
[rquote=490408&tid=76101&author=CuReUS][rquote=490395&tid=76101&author=kavu]
This b ...
14-8-2017 at 06:41
by: kavu
Geosmin synthesis
Accessing the proposed aldol product using this method is difficult. The Robinson annulation will no ...
13-8-2017 at 23:57
by: kavu
Identify This?
It's an Abderhalden's drying pistol. Nowadays a fairly obsolete piece of equipment.

The male join ...
16-6-2017 at 08:25
by: kavu
What is this Chemical?
Looks a lot like chromium(III)oxide and the reactivity profile would match as well. You could check ...
23-7-2016 at 00:49
by: kavu
Methylation of 1-iodo-2-naphthol
A quick reaxys search finds only two literature examples for methylating 1-iodo-2-naphthol, whereas ...
28-6-2016 at 00:43
by: kavu
Hydrochloric Acid: Mixture or Compound?
Your teacher is wrong and you are right. Hydrochloric acid is indeed the solution of dissociated and ...
25-8-2015 at 23:38
by: kavu
Grignard in presence of free OH
Interestingly enough silyl protected bromoethanols are not very commonly applied in grignard situati ...
19-8-2015 at 05:39
by: kavu
Grignard in presence of free OH
In the case of these deprotonation based "protections", which sometimes work, you have the problem o ...
16-8-2015 at 07:24
by: kavu
Grignard in presence of free OH
No, it is not. Grignard reagents (conjugate bases of alkanes) are much more basic than typical alcoh ...
14-8-2015 at 04:27
by: kavu
Handling Benzoyl Chloride?
Benzoyl chloride is not nearly as bad a lacrymathor as benzyl chloride. It just has a pungent, pecul ...
12-8-2015 at 02:34
by: kavu
What do you think about the Wikiversity ?
Wikis are in general not very good for learning stuff, they are good however for quick references. T ...
6-4-2015 at 00:58
by: kavu
diethylsulfide
I have had the displeasure of working with this particular thioether. The foul smell is very pungent ...
6-4-2015 at 00:53
by: kavu
Very First Step into Organic Chemistry
[rquote=399059&tid=61952&author=Loptr]
Yes, I know inorganic chemistry is what we first lea ...
30-3-2015 at 23:35
by: kavu
Very First Step into Organic Chemistry
[rquote=399038&tid=61952&author=aga]
What you Sith Masters are doing is carefully balancing ...
30-3-2015 at 01:10
by: kavu
Very First Step into Organic Chemistry
[rquote=398986&tid=61952&author=aga]
Some questions :-

If you're going to reflux with he ...
29-3-2015 at 23:52
by: kavu
my lab instructor...
Well, first of all NaBH4 is not all that sensitive to water, the reaction is reasonably slow. For ex ...
4-3-2015 at 03:25
by: kavu
Need help on amino alcohols
There are many perfectly good alpha-amination reactions, consider using them. This nucleophilic amin ...
31-8-2014 at 23:46
by: kavu
prepration of 1,6-dibromohexane
Well the IR and MS are doomed to be very similar. You really need to have a 1H and 13C NMRs done on ...
27-8-2014 at 01:36
by: kavu
Grignard reaction work up with concentrated sulfuric acid?
If the specific compound is not found try searching with similar structural motifs. In the case of h ...
25-7-2014 at 07:19
by: kavu
Is a Schlenk line absolutely necessary?
Most typical air/moisture sensitive reactions can be run without a Schlenk line. Assemble the appara ...
25-7-2014 at 04:47
by: kavu
Grignard reaction work up with concentrated sulfuric acid?
Barbier belongs to the "not in general" group, mosly I just wanted to emphasize this because the pro ...
25-7-2014 at 01:38
by: kavu
Grignard reaction work up with concentrated sulfuric acid?
in general zinc is not a suitable replacement for magnesium in grignard type reactions. Quenching an ...
25-7-2014 at 00:35
by: kavu
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